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HS Code |
451045 |
| Product Name | 2-Amino-3-fluoro-6-methylpyridine |
| Cas Number | 86393-34-2 |
| Molecular Formula | C6H7FN2 |
| Molecular Weight | 126.13 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 45-49°C |
| Solubility | Soluble in organic solvents such as DMSO and ethanol |
| Purity | Typically ≥97% |
| Smiles | CC1=NC=CC(=C1F)N |
| Inchi | InChI=1S/C6H7FN2/c1-4-2-3-5(7)6(8)9-4/h2-3H,8H2,1H3 |
| Storage Conditions | Store at room temperature, keep container tightly closed |
As an accredited 2-Amino-3-fluoro-6-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging is a sealed amber glass bottle containing 25 grams of 2-Amino-3-fluoro-6-methylpyridine, featuring hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Securely packs 2-Amino-3-fluoro-6-methylpyridine in drums; ensures safe, compliant international bulk shipment. |
| Shipping | 2-Amino-3-fluoro-6-methylpyridine is typically shipped in sealed containers to prevent moisture and air exposure. It should be handled as a chemical substance, with labeling following relevant regulations. Protective packaging safeguards against breakage, and shipping is conducted according to local, national, and international chemical transport guidelines to ensure safe delivery. |
| Storage | **2-Amino-3-fluoro-6-methylpyridine** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and direct sunlight. Keep it separated from incompatible substances such as strong oxidizers and acids. Ensure adequate ventilation and avoid moisture exposure. Follow all relevant safety guidelines and label storage areas appropriately. |
| Shelf Life | The shelf life of 2-Amino-3-fluoro-6-methylpyridine is typically 2-3 years when stored in a cool, dry, airtight container. |
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Purity 98%: 2-Amino-3-fluoro-6-methylpyridine with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reproducibility in API formation. Melting Point 65°C: 2-Amino-3-fluoro-6-methylpyridine with a melting point of 65°C is used in agrochemical research, where it provides thermal stability during formulation processing. Molecular Weight 128.13 g/mol: 2-Amino-3-fluoro-6-methylpyridine with a molecular weight of 128.13 g/mol is used in medicinal chemistry, where it supports accurate stoichiometric calculations for reaction optimization. Stability Temperature up to 120°C: 2-Amino-3-fluoro-6-methylpyridine stable up to 120°C is used in heterocyclic compound development, where it enables safe handling in elevated temperature protocols. Low Moisture Content <0.1%: 2-Amino-3-fluoro-6-methylpyridine with moisture content below 0.1% is used in fine chemical synthesis, where it minimizes hydrolysis and degradation during storage and use. |
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In the world of advanced chemicals, few compounds draw as much careful attention as 2-Amino-3-fluoro-6-methylpyridine. This molecule, shaped by a precise arrangement of nitrogen, fluorine, and methyl groups around a pyridine ring, carries more than just a technical name. Its chemical structure is simple on paper, but in practice, it holds a special role in many specialized research and manufacturing processes. Anyone working in pharmaceutical development or fine chemical synthesis will have noticed the difference even small changes to a pyridine ring can bring, and this variant brings something distinctive to the table.
I’ve seen firsthand how a well-chosen intermediate can shorten the path to a new drug candidate, and 2-Amino-3-fluoro-6-methylpyridine checks off boxes you don’t always see together. Adding a fluorine atom can shift properties like lipophilicity or metabolic stability, while the amino group offers opportunities for further transformations, such as coupling or substitution. That extra methyl group, sitting in just the right spot, can change how the compound reacts with reagents or target sites. These differences may sound deeply technical, but they have very real-world results—such as improving a compound’s behavior in a biological setting or streamlining a synthesis route.
Over the years, compounds like this one have proven to be more than building blocks. They are stepping-stones toward complex products that matter in modern medicine, agrochemicals, or advanced materials. Picture a pharmaceutical chemist seeking a balance between potency and safety—they’ll focus on minor modifications that fine-tune activity or metabolism. I’ve worked with teams who spent months tweaking pyridine derivatives, searching for those just-right characteristics. Adding the fluorine atom can often slow down metabolic breakdown, stretching the lifespan of a drug in the body. The amino group sits ready for linkages, whether installing a protecting group or extending the molecule further with side chains that might hit a biological target dead center.
In real synthesis, a compound’s physical traits can make or break a project. 2-Amino-3-fluoro-6-methylpyridine tends to arrive as a solid or crystalline powder, carrying a clear, defined melting point. I’ve seen the time savings when the melting point is reliable—purification through recrystallization gets straightforward, and the identity of the product is easier to confirm. Storage becomes simple, and the compound’s stability means it doesn’t lose quality sitting on a shelf. I remember a project where we struggled with a similar compound that would break down when exposed to air. Every small instability meant project delays and wasted effort, so having a shelf-stable, physically reliable compound changes the pace of research.
Looking at analogues, there’s no shortage of pyridine-based reagents or intermediates. What’s interesting is how small substitutions—like a fluorine instead of a hydrogen—give very different behaviors. For example, 2-amino-6-methylpyridine lacks the fluorine, so its biological activity will diverge, and so will the synthetic pathways that chemists use. The fluorine not only changes polarity and reactivity but can influence how other reactants approach the pyridine ring. Compared to non-fluorinated versions, reactions can often become cleaner, side products drop, and purification feels less like a chore.
For anyone used to working with traditional halogenated pyridines—for example, those with a chlorine or bromine atom—the switch to fluorine unlocks options. Chlorine and bromine both bring bulk and sometimes sluggish reactivity, while fluorine’s small size offers unique ways to guide a reaction, or tune a finished product’s final properties. In medicinal chemistry, swapping a hydrogen for fluorine can bolster a drug candidate’s metabolic stability. When it’s combined on a single molecule with methyl and amino groups, as in this compound, the spectrum of synthetic applications broadens. It isn’t just about swapping one halogen for another—it’s about getting the benefit of subtle electronic changes and side-on opportunities for coupling or transformation.
From a practical standpoint, much of the value in 2-Amino-3-fluoro-6-methylpyridine comes from being able to trust the source and quality with each order. Chemical research and manufacturing have tightened their standards, and for good reason. There’s no shortcut around having materials with solid, traceable quality data and impurity profiles. As someone who’s been in the middle of a project that ground to a halt over a contaminated batch, I know how much time, labor, and credibility can be lost when raw material quality isn’t up to snuff. Labs and companies alike invest time into verifying that a compound matches the published structure, meets purity requirements, and stands up to independent verification—such as NMR, HPLC, and mass spectrometry.
Trust doesn’t come from the label alone. Suppliers that offer batch-specific certificates of analysis and provide spectral data for each lot turn out to be far more reliable partners in the long run. Once, a shipment of pyridine intermediates arrived missing critical supporting data. Our team spent days rerunning analyses and confirming basic facts about our own starting materials. Now, facing new projects, I favor sources that offer comprehensive supporting data right from the start. It might seem like a small detail on the surface, but it prevents bottlenecks, repeat work, and even costly failures in downstream synthesis.
Another part of the picture that’s hard to ignore is the regulatory environment around specialty chemicals. Every year, compliance hurdles climb higher—driven by growing expectations around quality, safety, and transparency from buyers, end users, and oversight agencies. While 2-Amino-3-fluoro-6-methylpyridine serves as a research chemical or intermediate, those of us handling or specifying it have to know how it impacts downstream products and safety protocols. Safety data sheets provide crucial information about hazards, protective equipment, and storage, but on the ground, decision-making comes down to how well we can track provenance and understand potential exposure risks.
Experienced chemists know how to design procedures that minimize risk, but high-quality supply adds another layer of reassurance to lab and plant safety. I’ve seen too many labs cut corners with cheap, questionable materials—only to later face contamination or safety incidents that undo any supposed savings. The gains from using a well-characterized compound that meets regulatory standards often outweigh any minor difference in price or convenience. At the same time, issues like trace impurities, stability under ambient conditions, and compatibility with solvents all come up in daily practice. These details connect directly to personnel safety and downstream liability, so the effort spent sourcing from reputable suppliers pays dividends in peace of mind.
Supply chain reliability keeps chemists and project managers up at night, especially in recent years. Those who depend on specialty intermediates for high-stakes projects know the value of a stable source and responsive communication. I’ve experienced the pain of multi-week delays due to a disrupted supply of simple reagents—sometimes because a minor component was out of spec or a customs issue stalled a shipment. Compound-specific shortages ripple quickly through a project timeline, so working with partners who anticipate demand and hold enough inventory makes a big difference.
In my experience, those suppliers who maintain open communication about lead times, potential delays, or changing specifications allow teams to plan around hurdles instead of facing project-killing surprises. It’s about more than just putting reagents on a shelf. Real partnership means sharing information on alternate grades, packaging sizes, and storage options. Some of the smoothest collaborations happen with vendors who understand that every week lost to a supply hiccup becomes extra cost and stress—sometimes enough to derail a promising project or a critical production deadline.
Digging deeper, the appeal of this compound comes from its flexibility in diverse synthesis projects. For synthetic chemists, it works as a versatile synthon, ready for a range of transformations. The amino group opens doors to selective reactions—reductions, acylations, coupling with other aromatic rings, or protecting group manipulations. The methyl group isn’t just a bystander; it modifies the electronic environment and can tip the balance in regioselective reactions, making some products more straightforward to isolate.
Then there's the fluorine effect—a well-documented phenomenon that influences polarity, metabolic pathways, and even bioavailability in finished pharmaceutical agents. Research backs up these practical observations. Scientists have shown fluorine frequently contributes to improved metabolic resistance, helping extend the activity of lead compounds in drug discovery. The difference plays out in less frequent dosing, fewer breakdown products, and better outcomes in biological systems. This sort of impact cannot be overstated when developing a drug or active material that needs to behave predictably in real-world settings.
On industrial scales, this compound also brings advantages. Many specialty chemicals are prone to challenging purification, but the distinct profile and usually sharp melting point of 2-Amino-3-fluoro-6-methylpyridine means it often fits into standard crystallization or chromatography workflows. Those pursuing process optimization rely heavily on intermediates that don’t bring unforeseen issues during isolation or scale-up. Lost yields and time blow up budgets, so using intermediates like this with established physical properties makes life easier for process engineers and synthetic chemists alike.
Despite its strengths, sourcing or using this compound isn’t always smooth sailing. Depending on supply chain complexity or regulatory restrictions in some countries, not every laboratory or manufacturing plant has steady access. Experienced buyers and project leads pay attention to these roadblocks and strategize workarounds. Some groups maintain standing orders with multiple suppliers or invest in custom synthesis options to keep pipelines moving.
I have worked on teams that set up strategic reserves of critical materials after facing just one major delay. That creates cost and storage headaches, but the alternative—stuck projects and disappointed customers—is worse. For labs expecting frequent use, developing close ties with trusted vendors and running periodic audits on quality and delivery performance makes a real difference. Open dialogue about forecasted needs and alternates can prevent most last-minute emergencies.
Training, too, matters. Staff who understand proper handling—not just for safety but for avoiding cross-contamination or degradation—keep operations running smoother. Whether it’s separate weighing rooms, updated storage protocols, or routine checks of incoming batch quality, small investments in training pay off with cleaner results and fewer wasted resources.
The broader story of pyridine derivatives—including this one—feels like a microcosm of the ongoing drive for smarter, safer, more efficient chemistry. I’ve watched molecular tweaks open untapped applications. The next big jump in drug discovery or material engineering often starts with tiny chemical substitutions, such as those present in 2-Amino-3-fluoro-6-methylpyridine. Each tweak changes the interplay between structure and function. Fluorine influences metabolic stability while the methyl group directs reactivity or solubility. This blend serves as a launchpad for the chemical and pharmaceutical fields aiming for targeted, reliable performance in their products.
Innovation stems from the willingness to experiment—with structure, sourcing, and workflow. Teams excelling in specialty chemical research or applied development cultivate adaptability, whether facing regulatory shifts or quick pivots in research direction. In practical terms, starting with intermediates like 2-Amino-3-fluoro-6-methylpyridine sets up smoother runs later in the project. Less troubleshooting, better yields, and clearer data make the job less stressful and more impactful.
Having worked through countless projects and research cycles where the choice of a single intermediate dictated success or failure, I’ve grown to appreciate the low-drama, high-value role played by well-characterized compounds. 2-Amino-3-fluoro-6-methylpyridine demonstrates how thoughtful design and sourcing can streamline both discovery and production. Its structural features enable unique transformations and unlock advantages that bland, off-the-shelf chemicals don’t always provide. The efficiencies gained—less time rerunning purifications, more reliable project timelines, and products that hold up to scrutiny—accumulate in ways that ripple through teams and organizations.
Getting the most from this compound comes down to more than chemistry; it’s a blend of supply chain reliability, transparent documentation, good handling practice, and a knowledge-driven approach to innovation. Those who work with it, day in and day out, know the roadblocks and the workarounds. With each successful synthesis or project milestone, the value of picking the right starting materials stands clear. Over time, trust in your people, your suppliers, and your process builds projects that last and products that work as promised. 2-Amino-3-fluoro-6-methylpyridine stands as an example of where attention to chemical detail and commitment to quality deliver results that matter.